Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Jose Larumbe"'
Publikováno v:
Case Reports in Dermatological Medicine, Vol 2011 (2011)
Ablepharon syndrome is an extremely rare genetic problem that causes severe craniofacial deformities and numerous other abnormalities of the face, genitalia, and skin. The literature regarding this condition is scarce. We present a case of this syndr
Externí odkaz:
https://doaj.org/article/c8f8dda9c1164b1b82462130e87f1b73
Autor:
A. Rüya Yazici, S.A. Antonson, Rome Ocanto, Samira Alempour, Patrick C. Hardigan, Sandra Brener, Jose Larumbe, David Evans, Christie Michaud, Jude Crutchfield, Donald E. Antonson
Publikováno v:
The Journal of the American Dental Association. 143:115-122
Background Glass ionomer sealants are an alternative to resin-based sealants, especially for use in partially erupted permanent molars. The authors conducted a study to compare the retention, marginal staining and cariostatic properties of a glass io
Publikováno v:
The Cleft Palate-Craniofacial Journal. 42:1-6
Objective This report will discuss a new surgical technique for treating severe cases of macrocephaly in which the bony architecture is markedly distorted. The procedure relies on several novel surgical tools for its success that have not been previo
Autor:
Sibel A, Antonson, Donald E, Antonson, Sandra, Brener, Jude, Crutchfield, Jose, Larumbe, Christie, Michaud, A Rüya, Yazici, Patrick C, Hardigan, Samira, Alempour, David, Evans, Rome, Ocanto
Publikováno v:
Journal of the American Dental Association (1939). 143(2)
Glass ionomer sealants are an alternative to resin-based sealants, especially for use in partially erupted permanent molars. The authors conducted a study to compare the retention, marginal staining and cariostatic properties of a glass ionomer seala
Publikováno v:
Case Reports in Dermatological Medicine
Case Reports in Dermatological Medicine, Vol 2011 (2011)
Case Reports in Dermatological Medicine, Vol 2011 (2011)
Ablepharon syndrome is an extremely rare genetic problem that causes severe craniofacial deformities and numerous other abnormalities of the face, genitalia, and skin. The literature regarding this condition is scarce. We present a case of this syndr
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. 49(3)
Congenital microstomia in the newborn can result in poor functional and aesthetic outcomes. In the past, treatment options have included surgical methods such as commissurotomies and z-plasties as well as nonsurgical treatments using oral splints. In
Autor:
Steven Ellen, Daniel Arnold, Ines Velez, Diane Ede-Nichols, Victor Oramas, Melanie Bond, Jose Larumbe
Publikováno v:
The Journal of clinical pediatric dentistry. 34(1)
Hereditary Osteodystrophy, also called pseudohypoparathyroidism, Type 1A (PHP), is a very rare condition composed of a heterogeneous group of autosomal dominant disorders with the common feature of organ resistance to multiple hormones. These patient